4.7 Article

Chromosome 17q12-21 Variants Are Associated with Multiple Wheezing Phenotypes in Childhood

Journal

Publisher

AMER THORACIC SOC
DOI: 10.1164/rccm.202003-0820OC

Keywords

latent class analysis; genetics; 17q12-21; wheeze; asthma

Funding

  1. Cincinnati Childhood Allergy and Air Pollution Study: NIH [R01 ES11170, R01 ES019890]
  2. Columbia Center for Children's Environmental Health Cohort: NIH [P01 ES09600, R01 ES008977, P30ES09089, R01 ES013163]
  3. Environmental Protection Agency [R827027]
  4. Childhood Origins of Asthma [P01 HL070831, U10 HL064305, R01 HL061879]
  5. Epidemiology of Home Allergens and Asthma Study: NIH [R01 AI035786]
  6. Infant Immune Study [HL56177]
  7. Tucson Children's Respiratory Study [R01 HL132523]
  8. Urban Environment and Childhood Asthma [NO1AI25496, NO1 AI25482, HHSN272200900052C, HHSN272201000052I, RR00052, M01RR00533, UL1 RR025771, M01 RR00071, UL1 RR024156, UL1 TR001079, UL1RR024992, UL1TR000040]
  9. [UG3 OD023282]

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This study explored the association between wheezing phenotypes and 17q12-21 genetic variants in children, revealing four latent classes of wheezing and highlighting the genetic locus as relevant to wheezing. Differences in genetic associations between European American and African American children were also observed, suggesting potential racial/ancestral influences on wheezing phenotypes.
Rationale: Birth cohort studies have identified several temporal patterns of wheezing, only some of which are associated with asthma. Whether 17q12-21 genetic variants, which are closely associated with asthma, are also associated with childhood wheezing phenotypes remains poorly explored. Objectives: To determine whether wheezing phenotypes, defined by latent class analysis (LCA), are associated with nine 17q12-21 SNPs and if so, whether these relationships differ by race/ancestry. Methods: Data from seven U.S. birth cohorts (n = 3,786) from the CREW (Children's Respiratory Research and Environment Workgroup) were harmonized to represent whether subjects wheezed in each year of life from birth until age 11 years. LCA was then performed to identify wheeze phenotypes. Genetic associations between SNPs and wheeze phenotypes were assessed separately in European American (EA) (n = 1,308) and, for the first time, in African American (AA) (n = 620) children. Measurements and Main Results: The LCA best supported four latent classes of wheeze: infrequent, transient, late-onset, and persistent. Odds of belonging to any of the three wheezing classes (vs. infrequent) increased with the risk alleles for multiple SNPs in EA children. Only one SNP, rs2305480, showed increased odds of belonging to any wheezing class in both AA and EA children. Conclusions: These results indicate that 17q12-21 is a wheezing locus, and this association may reflect an early life susceptibility to respiratory virusescommon to all wheezing children. Which children will have their symptoms remit or reoccur during childhood may be independent of the influence of rs2305480.

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